Autosomal Dominant Gyrate Atrophy-Like Choroidal Dystrophy Revisited: 45 Years Follow-Up and Association with a Novel C1QTNF5 Missense Variant
暂无分享,去创建一个
V. Marino | D. Dell’Orco | U. Kellner | N. Weisschuh | Karin Schäferhoff | S. Weinitz | Ghazaleh Farmand | P. Mazzola | F. Kortüm | Sebastian Deutsch